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Controlled Radical Polymerization of Methacrylic Monomers in the Presence of a Bis(ortho-chelated) Arylnickel(II) Complex and Different Activated Alkyl Halides

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TLDR
In this article, a novel class of homogeneous nickel(II) catalysts, denoted as Ni(NCN)Br, is reported to mediate in the presence of activated alkyl halides, e.g., CCl4 or α-halocarbonyl compounds, and remarkably enough, poly(methyl methacrylate) (PMMA) with molecular weight up to at least 105 g/mol was synthesized in a controlled fashion.
Abstract
A novel class of homogeneous nickel(II) catalysts, i.e [Ni{o,o‘(CH2NMe2)2C6H3}Br], denoted as Ni(NCN‘)Br, is reported to mediate in the presence of activated alkyl halides, e.g., CCl4 or α-halocarbonyl compounds, a well-controlled radical polymerization of methacrylic monomers [methyl and n-butyl methacrylate), (MMA, n-BuMA)] at rather low temperatures (<100 °C). The number-average molecular weight of the polymer gradually increased with the monomer conversion and was inversely proportional to the initiator concentration of alkyl halides. The molecular weight distribution (MWD) remained very narrow during the whole course of the polymerization (MWD < 1.3). All the experimental data including a successful block copolymerization (n-BuMA-b-MMA) experiment were in agreement with a living polymerization process, and remarkably enough, poly(methyl methacrylate) (PMMA) with molecular weight up to at least 105 g/mol was synthesized in a controlled fashion. Increased thermal stability of the PMMA is a further indi...

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Citations
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Journal ArticleDOI

Mn2(CO)10-Induced RAFT Polymerization of Vinyl Acetate, Methyl Acrylate, and Styrene

TL;DR: In this paper, a dinuclear manganese complex [Mn2(CO)10] induced the controlled/living radical polymerization of various conjugated and unconjugated vinyl monomers including vinyl acetate, methyl acrylate, and styrene in conjunction with dithiocarbonyl compounds [R-SC(S)Z] under weak visible light at 40 °C.
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Controlled/“living” radical polymerization of styrene catalyzed by FeCl2/succinic acid

TL;DR: In this paper, a new ligand, succinic acid, was successfully used for atom transfer radical polymerization, which was carried out at 40 to 100°C in bulk with α-bromoethyl benzene as the initiator and FeCl 2 /(succinic acid) as the catalyst system.
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Interaction of Propagating Radicals with Copper(I) and Copper(II) Species

TL;DR: Results indicate that control in ATRP does not originate in interactions of growing radicals with copper complexes but in the reversible halogen atom transfer.
Journal ArticleDOI

Inner sphere and outer sphere electron transfer reactions in atom transfer radical polymerization

TL;DR: In this paper, the participation of electron transfer (ET) processes in atom transfer radical polymerization (ATRP) is discussed, which includes the homolytic cleavage of C-halogen bond in dormant macromolecular alkyl halides species by the Cu(I) activator with the rate constant k −100±1 M−1s−1.
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Reversible addition-fragmentation chain transfer polymerization of methyl methacrylate in suspension

TL;DR: In this paper, the reversible addition-fragmentation chain transfer polymerization of methyl methacrylate mediated by 2-cyanoprop-2-yl dithiobenzoate (CPDB) in bulk and suspension was studied, and in both polymerization systems, a good control of the molecular weight and polydispersity was observed.
References
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Journal ArticleDOI

Narrow molecular weight resins by a free-radical polymerization process

TL;DR: In this paper, free radical polymerization was used to obtain polystyrene and poly(styrene-co-butadiene) with narrow polydispersity (1.19-1.36) in the presence of 2,2,6, 6,6-tetramethyl-1-piperidinyloxy using benzoyl peroxide as initiator
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Controlled Living Radical Polymerization - Halogen Atom-Transfer Radical Polymerization Promoted by a Cu(I)Cu(II) Redox Process

TL;DR: An extension of ATRA to atom transfer radical addition, ATRP, provided a new and efficient way to conduct controlled/living radical polymerization as mentioned in this paper, using a simple alkyl halide, R-X (X = Cl and Br), as an initiator and a transition metal species complexed by suitable ligand(s), M t n /L x, e.g., CuX/2,2'-bipyridine, as a catalyst.
Journal ArticleDOI

|[lsquo]|Living|[rsquo]| Polymers

M. Szwarc
- 24 Nov 1956 - 
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